Canonical Allele Identifier: CA15638468
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs10510110

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122432914T>C , CM000672.2:g.122432914T>C GRCh38
NC_000010.10:g.124192430T>C , CM000672.1:g.124192430T>C GRCh37
NC_000010.9:g.124182420T>C NCBI36
NG_027823.1:g.63337T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000368990.7:c.*2976T>C ENSP00000357986.3:p.=